ACTD- ASEAN
Download as PPTX, PDF37 likes26,009 views
The document discusses the ASEAN Common Technical Dossier (ACTD) format for pharmaceutical product registration applications submitted to ASEAN regulatory authorities. The ACTD format aims to standardize applications to reduce submission time and resources while facilitating regulatory review. It includes four parts covering administrative data, quality, nonclinical, and clinical information. The ACTD guideline describes the sections within each part, including overviews, summaries, study reports, and references. The standard format seeks to provide a consistent and transparent presentation of technical information to support evaluation and understanding of registration applications.
ACTD- ASEAN
- 1. ACTD : ASEAN COMMON TECHNICAL DOCUMENT AND REGULATORY MANAGEMENT PREPARED BY : NAILA KANWAL Senior Officer Regulatory Affairs. The SEARLE Company Limited
- 2. CONTENT 1- DOSSIER a)Dossiers and Regulatory Affairs b)Features c)Benefits d)Applications 2- AEC (ASEAN Economic Community) 3- ASEAN COUNTRIES 4- ASEAN REQUIREMENT a)Agreed ACTR, ACTD, Technical guidelines b) Objective 5- ASEAN COMMON TECHNICAL DOSSIER a) Preamble b) Sections of ASEAN Common technical dossier c) ACTD Guideline
- 3. DOSSIER It s a complete set of document. •A collection of papers giving detailed information about a particular person or subject. Dossier and Regulatory Affairs : Dossier helps , •To create, assemble, update and publish a composite document(s) from various individual document sources and formats. •A compound document is resulting from a dynamic merge and assembly of elementary documents monitored by a structuring and publishing agent (the Dossier module). •Elementary documents might be of heterogeneous types and formats. They should be managed as a whole. For instance, a training manual can be made up of Word documents, Powerpoint presentations, Excel spreadsheets . It is published and made available to all users as a single document.
- 4. Dossier and Regulatory Affairs : • All documents are managed as a single, consistent, structured and unified document. No more time wasted on assembling and maintaining a constantly moving document means immediate return on investment. •Each document or sub dossier follows its own lifecycle. Individual changes update in real time the whole dossier. •Dossier allows various combinations of the same content in order to adapt to different contexts or targets: FDA approval, other regulatory approval, suppliers/customers needs, auditing purposes, etc.
- 7. APPLICATIONS: • For registration of Pharmaceutical Products. •In Local market. •In International market. For renewal of registration of Pharmaceutical Products.
- 10. ASEAN COUNTRIES ASEAN Leader Summit ASEAN Economic Community (AEC) “by the year 2015….. ASEAN will be Single Market and Single Production Base 1- Free flow of Goods 2- Free flow of Services 3- Free flow of Investment 4- Free flow of Capitals 5-Free flow of Skilled Labour
- 12. ASEAN REQUIREMENT Agreed “ACTR, ACTD, Technical guidelines” ACTR (ASEAN Common Technical Requirement) ACTD (ASEAN Common Technical Dossier) Technical “Quality, Safety, Efficacy” guidelines - -adopted guidelines (from WHO, ICH, and International pharmacopoeia) Objective: To develop harmonization scheme of Pharmaceuticals regulations of the ASEAN member countries, to complement and facilitate the objective of AFTA, particularly, the elimination of Technical Barriers to Trade posed by the regulations, without compromising on drug quality, efficacy, and safety” & facilitate the AEC !!!!
- 13. ASEAN COMMON TECHNICAL DOSSIER PREAMBLE This ASEAN Common Technical Dossier (ACTD) is a guideline of the agreed upon common format for the preparation of a well- structured Common Technical Dossier (CTD) applications that will be submitted to ASEAN regulatory authorities for the registration of pharmaceuticals for human use. This guideline describes a CTD format that will significantly reduce the time and resources needed to compile applications for registration and in the future, will ease the preparation of electronic documental submissions. Regulatory reviews and communication with the applicant will be facilitated by a standard document of common elements.
- 14. ASEAN COMMON TECHNICAL DOSSIER This guideline merely demonstrates an appropriate write-up format for acquired data. However, applicants can modify, if needed, to provide the best possible presentation of the technical information, in order to facilitate the understanding and evaluation of the results upon pharmaceutical registration. Throughout the ACTD, the display of Information should be unambiguous and transparent, in order to facilitate the review of the basic data and to help a reviewer become quickly oriented to the application contents. Text and tables should be prepared using margins that allow the document to be printed on either A4 or 8.5 x 11 paper.
- 15. ASEAN COMMON TECHNICAL DOSSIER The left-hand margin should be sufficiently large that information is not obscured by the method of binding. Font and size, (Times New Roman, 12-point font), for text and tables should be of a style andsize that are large enough to be easily legible, even after photocopying. Every page should be numbered, with the first page of each part designated as page 1. For a paper, Common Technical Acronyms and abbreviations should be defined the first time they are used In each part.
- 16. SECTIONS OF ASEAN COMMON TECHNICAL DOSSIER The Common Technical Document is organized into four parts as follows: Part I. Table of Contents, Administrative Data and Product Information. Part I contains initially the overall Table of Contents of the whole ACTD to provide basicaly the informations that could be looked through respectively. Secondly, the next content is the Administrative Data where required specific documentation in details is put together such as application forms, label, package insert etc. The last section of this part is Product Information where necessary information includes prescribed information, mode of action, side effects etc. A general introduction to the pharmaceutical, including its pharmacologic class and mode of action should be included.
- 17. SECTIONS OF ASEAN COMMON TECHNICAL DOSSIER Part II. Quality Document Part II should provide the Overall Summary followed by the Study Reports. The quality control document should be described in details as much as possible. Part III. Nonclinical Document Part III should provide the Nonclinical Overview, followed by the Nonclinical Written Summaries and the Nonclinical Tabulated Summaries. The document of this part is not required for Generic Products, Minor Variation Products and some Major Variation Products. For ASEAN member countries, the Study Reports of this part may not be required for NCE, Biotechnological Products and other Major Variation Products if the Original Products are already registered and approved for market authorization in Reference Countries. Therefore, the authority who requires specific Study Reports should ask for the necessary documents.
- 18. SECTIONS OF ASEAN COMMON TECHNICAL DOSSIER Part IV Clinical Document Part IV should provide the Clinical Overview and the Clinical Summary. The document of this part is not required for Generic Products, Minor Variation Products and some Major Variation Products. For ASEAN member countries, the Study Reports of this part may not be required for NCE, Biotechnological Products and other Major Variation Products if the Original Products are already registered and approved for market authorization in Reference Countries. Therefore, the authority who requires specific Study Reports should ask for the necessary documents.
- 19. ASEAN COMMON TECHNICAL DOSSIER GUIDELINE Part I: Table of Content Administrative Information and Prescribing Information Section A: Introduction Section B: Overall ASEAN Common Technical Dossier Table of Contents Section C: Documents required for registration (for example, application forms, labelling, Product Data Sheet, prescribing information)
- 20. ASEAN COMMON TECHNICAL DOSSIER GUIDELINE Part II: Quality Document Section A: Table of Contents Section B: Quality Overall Summary Section C: Body of Data Part III: Nonclinical Document Section A: Table of Contents Section B: Nonclinical Overview Section C: Nonclinical Written and Tabulated Summaries . ` 1-Table of Contents 2. Pharmacology 3. Pharmacokinetics 4. Toxicology
- 21. ASEAN COMMON TECHNICAL DOSSIER GUIDELINE Section D: Nonclinical Study Reports 1. Table of Contents 2. Pharmacology 3. Pharmacokinetics 4. Toxicology Part IV: Clinical Document Section A: Table of Contents Section B: Clinical Overview Section C: Clinical Summary 1. Summary of Biopharmaceutics and Associated Analytical Methods 2. Summary of Clinical Pharmacology Studies 3. Summary of Clinical Efficacy 4. Summary of Clinical Safety 5. Synopses of Individual Studies
- 22. ASEAN COMMON TECHNICAL DOSSIER GUIDELINE Section D: Tabular Listing of All Clinical Studies Section E: Clinical Study Reports Section F: List of Key Literature References
- 23. ASEAN COMMON TECHNICAL DOSSIER